PSF Regulates the Porcine P450scc IFGRE

PSF 监管猪 P450scc IFGRE

• 批准号: 7901051
• 负责人: Randall J Urban
• 金额: $ 23.19万
• 依托单位: UNIVERSITY OF TEXAS MED BR GALVESTON
• 依托单位国家: 美国
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-12-01 至 2011-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7901051
• 关键词: Affect; Aromatase; Binding; Cell Line; Cell membrane; Cells; Cholesterol; Complex; Cytochrome P450; Data; Disease; Enzymes; Family suidae; Future; Gene Expression; Gene Expression Regulation; Genes; Genetic Transcription; Gonadotropins; Hormonal; Hormones; Insulin-Like Growth Factor I; Knowledge; Lead; Mediating; Mus; Nuclear; Nucleic Acid Regulatory Sequences; Ovarian; Ovary; PTB-associated splicing factor; Pathway interactions; Phosphorylation; Phosphorylation Site; Phosphotransferases; Polycystic Ovary Syndrome; Polymerase; Polypyrimidine Tract-Binding Protein; Publications; RNA; Regulation; Repression; Reproductive Endocrinology; Response Elements; Retrotransposon; Side; Signal Pathway; Signal Transduction; Steroid biosynthesis; Threonine; Validation; Work; atypical protein kinase C; granulosa cell; novel; overexpression; prevent; protein kinase C iota; protein protein interaction; reproductive; research study; tool; transcription factor

DESCRIPTION (provided by applicant): Our work focuses on IGF-I regulation of gene expression for P-450 cholesterol side-chain cleavage (P450scc), the rate-limiting enzyme in the steroidogenic pathway. We identified an IGF-I response element (IGFRE) of the porcine P450scc gene that binds Sp1(stimulator) and polypyrimidine tract-binding protein (PTB)-associated splicing factor (PSF, repressor). In this proposal we will investigate mechanisms of PSF regulation of IGFRE activity. Studies will be conducted in a stable porcine granulosa cell line, the JC-410 cells. We hypothesize that PSF repression of the IGFRE involves a mechanism that prevents IGF-I-stimulated phosphorylation of Sp1. In specific aim 1 we will determine IGF-I-mediated Sp1 phosphorylation sites having already demonstrated that IGF-I stimulates phosphorylation of threonine 739 on Sp1, a known erk 1/2 phosphorylation site. In specific aim 2 we will investigate the erk 1/2 signaling pathway as at least a partial mechanism for regulating IGF-I stimulation of the IGFRE through Sp1 phosphorylation. Finally, we will investigate protein kinase C (PKC) iota as a modulator of PSF-Sp1 interactions regulating the IGFRE (specific aim 3). We will determine the fundamental mechanisms whereby IGF-I controls P450scc gene expression through interactions of Sp1, PSF, and PKC iota. This knowledge will increase our understanding and provide the basic background for novel concepts on hormonal control of ovarian steroidogenesis.

描述（由申请人提供）：我们的工作重点是IGF-I对P-450胆固醇侧链裂解（P450 SCC）基因表达的调控，P450 SCC是类固醇生成途径中的限速酶。我们确定了猪P450 SCC基因的IGF-I反应元件（IGFRE），其结合Sp1（刺激物）和多聚嘧啶片段结合蛋白（PTB）相关剪接因子（PSF，阻遏物）。 在这个提议中，我们将研究PSF调节IGFRE活性的机制。研究将在稳定的猪颗粒细胞系JC-410细胞中进行。我们推测PSF对IGFRE的抑制涉及一种阻止IGF-I刺激的Sp1磷酸化的机制。在具体目标1中，我们将确定IGF-I介导的Sp1磷酸化位点，已经证明IGF-I刺激Sp1上的苏氨酸739磷酸化，这是一个已知的erk 1/2磷酸化位点。在具体目标2中，我们将研究erk 1/2信号通路作为通过Sp1磷酸化调节IGF-I刺激IGFRE的至少部分机制。最后，我们将研究蛋白激酶C（PKC）iota作为PSF-Sp1相互作用调节IGFRE的调节剂（具体目标3）。 我们将确定IGF-I通过Sp1、PSF和PKC iota的相互作用控制P450 SCC基因表达的基本机制。这些知识将增加我们的理解，并为卵巢类固醇激素生成的激素控制的新概念提供基本背景。